Canonical Allele Identifier: CA1396762294

Gene: GSK3B

Linked Data

• dbSNP Id: rs2056508130

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119892014_119892015del , CM000665.2:g.119892014_119892015del	GRCh38
NC_000003.11:g.119610861_119610862del , CM000665.1:g.119610861_119610862del	GRCh37
NC_000003.10:g.121093551_121093552del	NCBI36
NG_012922.1:g.207403_207404del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264235.13:c.813+13740_813+13741del MANE Select	ENSP00000264235.9:n.813+13740_813+13741del
ENST00000316626.6:c.813+13740_813+13741del	ENSP00000324806.5:n.813+13740_813+13741del
ENST00000650344.2:c.813+13740_813+13741del	ENSP00000497956.2:n.813+13740_813+13741del
ENST00000676566.1:n.639+13740_639+13741del
ENST00000676887.1:c.132-15507_132-15506del	ENSP00000502977.1:n.132-15507_132-15506del
ENST00000676948.1:c.154+8543_154+8544del
ENST00000677046.1:c.98+13740_98+13741del
ENST00000677069.1:c.99-11517_99-11516del
ENST00000677362.1:c.107+20689_107+20690del
ENST00000677483.1:c.99-9181_99-9180del
ENST00000677502.1:n.596+13740_596+13741del
ENST00000677648.1:c.99-11505_99-11504del
ENST00000677716.1:c.131+24029_131+24030del	ENSP00000503671.1:n.131+24029_131+24030del
ENST00000677788.1:n.1283-11517_1283-11516del
ENST00000677995.1:c.326+13740_326+13741del	ENSP00000504203.1:n.326+13740_326+13741del
ENST00000678013.1:c.98+13740_98+13741del
ENST00000678181.1:c.85-28410_85-28409del	ENSP00000504266.1:n.85-28410_85-28409del
ENST00000678377.1:c.229+13740_229+13741del	ENSP00000503164.1:n.229+13740_229+13741del
ENST00000678439.1:c.813+13740_813+13741del	ENSP00000503868.1:n.813+13740_813+13741del
ENST00000678509.1:c.99-9181_99-9180del
ENST00000678561.1:c.486+13740_486+13741del	ENSP00000503494.1:n.486+13740_486+13741del
ENST00000678754.1:n.99-7633_99-7632del
ENST00000678787.1:c.195-15507_195-15506del
ENST00000679066.1:c.85-15507_85-15506del	ENSP00000503626.1:n.85-15507_85-15506del
ENST00000679188.1:c.112-15507_112-15506del	ENSP00000504252.1:n.112-15507_112-15506del
ENST00000679194.1:c.108-15507_108-15506del
ENST00000679206.1:c.131+24029_131+24030del	ENSP00000502943.1:n.131+24029_131+24030del
ENST00000264235.12:c.813+13740_813+13741del	ENSP00000264235.8:n.813+13740_813+13741del
ENST00000316626.5:c.813+13740_813+13741del	ENSP00000324806.5:n.813+13740_813+13741del
NM_001146156.1:c.813+13740_813+13741del	NP_001139628.1:n.813+13740_813+13741del
NM_002093.3:c.813+13740_813+13741del	NP_002084.2:n.813+13740_813+13741del
XM_006713610.1:c.813+13740_813+13741del	XP_006713673.1:n.813+13740_813+13741del
XM_006713611.1:c.813+13740_813+13741del	XP_006713674.1:n.813+13740_813+13741del
NM_001354596.1:c.813+13740_813+13741del	NP_001341525.1:n.813+13740_813+13741del
XM_006713610.3:c.813+13740_813+13741del	XP_006713673.1:n.813+13740_813+13741del
NM_001146156.2:c.813+13740_813+13741del MANE Select	NP_001139628.1:n.813+13740_813+13741del
NM_001354596.2:c.813+13740_813+13741del	NP_001341525.1:n.813+13740_813+13741del
NM_002093.4:c.813+13740_813+13741del	NP_002084.2:n.813+13740_813+13741del